Patricia O'Lague

Inherited Chondrodysplasia Punctata Due to a Deletion of the Terminal Short Arm of an X Chromosome

Cynthia J. Curry, R. Ellen Magenis, Michael G. Brown et al. · New England Journal of Medicine · 1984 · 191 citations

Life Sciences, Genetics, Molecular Genetics +17

Mild autosomal dominant hypophosphatasia: In utero presentation in two families

Cynthia A. Moore, Cynthia J. Curry, Paula S. Henthorn et al. · American Journal of Medical Genetics · 1999 · 75 citations

Medicine, Endocrinology, Genetics +16

De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing

Samuel P. Strom, Reymundo Lozano, Hane Lee et al. · BMC Medical Genetics · 2014 · 63 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.

Alain Verloès, Cynthia J. Curry, M Jamar et al. · Journal of Medical Genetics · 1998 · 44 citations · Full text

Medicine, Clinical Sciences, Pediatrics +13